chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	105075249	105075250	T	C	26	GENIC	heterozygous	118508725
13	105075257	105075258	T	G	26	GENIC	heterozygous	118508726
13	105075282	105075283	C	G	34	GENIC	heterozygous	118508727
13	105075359	105075360	T	A	23	GENIC	heterozygous	118508728
13	105080773	105080774	T	C	148	GENIC	heterozygous	118508741
13	105080784	105080785	T	C	151	GENIC	heterozygous	118467869
13	105080807	105080808	T	C	170	GENIC	heterozygous	118467870
13	105080873	105080874	C	T	121	GENIC	heterozygous	118467872
13	105081088	105081089	C	T	156	GENIC	heterozygous	118551472
13	105081099	105081100	C	T	185	GENIC	heterozygous	118595010
13	105081335	105081336	A	G	89	GENIC	heterozygous	118467874
13	105081438	105081439	G	C	71	GENIC	heterozygous	118467877
13	105081508	105081509	C	T	173	GENIC	heterozygous	118467878
13	105095630	105095631	G	A	57	GENIC	heterozygous	118508753
13	105096950	105096951	C	A	166	GENIC	heterozygous	118595012
13	105098508	105098509	C	T	162	GENIC	heterozygous	118583111
13	105130038	105130039	G	T	70	GENIC	heterozygous	118529937
13	105109162	105109163	G	A	51	GENIC	homozygous	114438230
13	105101262	105101263	T	C	47	GENIC	possibly homozygous	114438228